Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene

Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism

(2011) Danuta Z Loesch et al.   GENETICS IN MEDICINE

Aging in fragile X syndrome

(2010) Agustini Utari et al.   Journal of Neurodevelopmental Disorders

Early onset of neurological symptoms in fragile X premutation carriers exposed to neurotoxins

(2010) Ripon Paul et al.   NEUROTOXICOLOGY

The Korsakoff Syndrome: Clinical Aspects, Psychology and Treatment

(2009) M. D. Kopelman et al.   ALCOHOL AND ALCOHOLISM

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

(2009) DZ Loesch et al.   CLINICAL GENETICS

Alcohol-induced changes in the brain as assessed by MRI and CT

(2009) Sasikhan Geibprasert et al.   EUROPEAN RADIOLOGY

Examination of FMR1 transcript and protein levels among 74 premutation carriers

(2009) Emmanuel Peprah et al.   JOURNAL OF HUMAN GENETICS

Neuroimaging of the Wernicke-Korsakoff Syndrome

(2008) E. V. Sullivan et al.   ALCOHOL AND ALCOHOLISM

Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations

(2008) Elisabetta Tabolacci et al.   EUROPEAN JOURNAL OF HUMAN GENETICS